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Öğe Benign metastasizing leiomyoma(Springer, 2008) Sapmaz, Feride; Ergin, Makbule; Katrancioglu, Ozgur; Gonlugur, Tanseli; Gonlugur, Ugur; Elagoz, SahendeA 41-year-old woman presented with chest pain and a cough. There was a solitary pulmonary nodule in the upper-left lobe. The patient had no history of neoplasm except a hysterectomy for uterine leiomyoma five years before. Six months after the first presentation, the tumor showed a gradual increase in size; an explorative thoracotomy was performed. The histopathologic examination showed a tumor consisting of well-differentiated spindle-shaped cells with intervening collagen. She was readmitted 8 months after the operation because of right-sided spontaneous pneumothorax. Multiple pulmonary nodules appeared when the lung was re-expanded by chest tube drainage. In conclusion, uterine leiomyomas can metastasize to various organs, such as lungs, despite having a benign pathologic appearance.Öğe Differential diagnosis of a cavitary lung lesion in 45-year old man(2011) Gönlügür, Tanseli; Sapmaz, Feride; Gönlügür, Uğur; Elagöz, ŞahendeAkciğer kaviteleri enfeksiyöz ve non-enfeksiyöz nedenlerle gelişebilir. Kırk-bir yaşında erkek, bir hafta süren prudüktif öksürük ve göğüste pleural ağrı ile başvurdu ve hastaneye yatırıldı. Göğüs bilgisayarlı tomografisi sol üst lobda kaviter bir lezyonu gösterdi. Açık lob biyopsisi alveoller ve bronşiyoller içinde bağ dokusu varlığını gösterdi. Sonuç olarak hastaya nadir bir akciğer kavite yapıcı lezyon nedeni olana kriptojenik organizan pnömoni tanısı kondu. Olgu kaviter lezyonlarda tüberkülozla birlikte bu tür nadir nedenlerin de ayırıcı tanıda düşünülmesi gerektiğini vurgulamak için sunuldu.Öğe Intraosseous Lipoma of the Rib(Elsevier Science Inc, 2009) Katrancioglu, Ozgur; Sapmaz, Feride; Gonlugur, Tanseli E.; Elagoz, Sahande; Gonlugur, Ugur[Anstract Not Available]Öğe Pulmonary lymphangitic sarcomatosis and a review of the literature(Springer, 2009) Gonlugur, Tanseli; Sapmaz, Feride; Katrancioglu, Ozgur; Gonlugur, Ugur; Elagoz, SahendeIntrapulmonary spread of a sarcoma via lymphatics is a rare cause of death in a young adult. A 31-year old man was admitted to our hospital complaining of dyspnea and malaise of 2 months' duration. A chest radiography revealed bilateral hilar enlargement, and reticulonodular infiltrations. Thoracic CT-scans demonstrated mediastinal lymphadenopathy, thickening of interlobular septa, polygonal lines, and thickening of bronchovascular bundles. The diagnosis was made by open-lung biopsy. The patient died within 3 months after diagnosis. Pulmonary lymphangitic sarcomatosis is a rare but important manifestation of an angiosarcoma. Optimal treatment of these patients is not well defined, but a trial of chemotherapy may be warranted.